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Development of a nomogram model to predict survival outcomes in patients with primary hepatic neuroendocrine tumors based on SEER database

机译:基于SEER数据库的基于SER数据库的肝脏神经内分泌肿瘤患者预测生存结果的载体模型

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Primary hepatic neuroendocrine tumors (PH-NETs) are extremely rare and unknown. Because of its rarity, its prognosis features and influencing factors are not well established. Data of 140 patients with PH-NETs diagnosed in the SEER database from 1975 to 2016 were collected. The demographics and clinic-pathological features were described. By using propensity-score matching (PSM) analysis, three associated cohorts were selected to describe the malignancy of PH-NETs and univariate analysis was conducted. Then, multivariate Cox analyses were performed and a predicting nomograph was constructed. C-index, receiver operating characteristic (ROC) curve and calibration curves were used to evaluate the predictive value of nomogram. The overall survival outcomes of PH-NETs were superior to hepatocellular carcinoma (HCC) with a mean survival time 30.64 vs 25.11?months (p?=?0.052), but inferior to gastrointestinal tract neuroendocrine tumors in situ (GI-NETs in situ) with a mean survival time 30.64 vs 41.62?months (p?=?0.017). With reference to gastrointestinal neuroendocrine tumors with liver metastasis (GI-NETs-LM), GI-NETs-LM had better outcomes in short time (1-year survival rate: 64.75% vs 56.43%) but was worse in long time (5-year survival rate: 8. 63% vs 18.57%). Multivariate Cox analyses showed that tumor grade and surgery were two independent factors for prognosis of the patients (p??0.00). Tumor grade and surgery were used to construct the predicting nomogram. The C-index was 0.79 (95%CI?=?0.75–0.83). The area under curve (AUC) values in ROC were 0.868 in 1-year and 0.917 in 3-year survival and the calibration curves showed good consistency. The overall prognosis PH-NETs is generally favorable, better than HCC and GI-NETs-LM in long term. Preoperative biopsy and complete pathological diagnosis were recommended. Radical surgical intervention including transplantation was the first choice in PH-NETs therapy.
机译:原发性肝神经内分泌肿瘤(pH型网)非常罕见和未知。由于其罕见,其预后特征和影响因素并不明确。收集了1975年至2016年在SEER数据库中诊断出的140例pH-蚊帐的数据。描述了人口统计学和临床​​病理特征。通过使用倾向评分匹配(PSM)分析,选择了三个相关的群组来描述pH-Nets的恶性肿瘤,并进行单变量分析。然后,进行多变量COX分析,构建预测的提示标记。 C折射率,接收器操作特性(ROC)曲线和校准曲线用于评估墨顶图的预测值。 pH-net的整体存活结果优于肝细胞癌(HCC),平均存活时间为30.64 vs 25.11?月份(p?= 0.052),但差不多到原位的胃肠道神经内分泌肿瘤(原位上的Gi-net)平均存活时间30.64 vs 41.62?月份(p?= 0.017)。参照肝脏转移(GI-Nets-LM)的胃肠神经内分泌肿瘤,GI-Nets-LM在短时间内具有更好的结果(1年生存率:64.75%Vs 56.43%),但在很长一段时间内更糟糕(5-年生存率:8. 63%与18.57%)。多变量Cox分析表明,肿瘤等级和手术是患者预后的两个独立因素(p?& 0.00)。肿瘤级和手术用于构建预测的墨迹图。 C折射率为0.79(95%CI?= 0.75-0.83)。 ROC曲线(AUC)值下的区域为0.868,在1年内,3年生存率为0.917,校准曲线显示出良好的一致性。总预后pH网通常优于HCC和长期GI-Nets-LM。建议术前活检和完全病理诊断。包括移植的激进手术干预是pH-Nets治疗中的第一选择。

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